ENST00000225964.10:c.3124G>T
MANE Select
|
ENSP00000225964.6:p.Ala1042Ser
|
|
ENST00000225964.9:c.3124G>T
|
ENSP00000225964.5:p.Ala1042Ser
|
|
ENST00000511732.1:n.68G>T
|
|
|
NM_000088.3:c.3124G>T , LRG_1t1:c.3124G>T
|
NP_000079.2:p.Ala1042Ser
|
|
XM_005257058.3:c.2854G>T
|
XP_005257115.2:p.Ala952Ser
|
|
XM_005257059.3:c.2206G>T
|
XP_005257116.2:p.Ala736Ser
|
|
XM_011524341.1:c.2926G>T
|
XP_011522643.1:p.Ala976Ser
|
|
XM_005257058.4:c.2854G>T
|
XP_005257115.2:p.Ala952Ser
|
|
XM_005257059.4:c.2206G>T
|
XP_005257116.2:p.Ala736Ser
|
|
NM_000088.4:c.3124G>T
MANE Select
|
NP_000079.2:p.Ala1042Ser
|
|